US20220016002A1 - Non-aluminium antiperspirant compositions - Google Patents

Non-aluminium antiperspirant compositions Download PDF

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Publication number
US20220016002A1
US20220016002A1 US17/297,836 US201917297836A US2022016002A1 US 20220016002 A1 US20220016002 A1 US 20220016002A1 US 201917297836 A US201917297836 A US 201917297836A US 2022016002 A1 US2022016002 A1 US 2022016002A1
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US
United States
Prior art keywords
composition
weight
amphiphilic material
volatile silicone
ethanol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
US17/297,836
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English (en)
Inventor
Philip Christopher Waterfield
Aneliya Nikolova Zdravkova
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Conopco Inc
Original Assignee
Conopco Inc
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Filing date
Publication date
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Assigned to CONOPCO, INC., D/B/A UNILEVER reassignment CONOPCO, INC., D/B/A UNILEVER ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: WATERFIELD, PHILIP CHRISTOPHER, ZDRAVKOVA, ANELIYA NIKOLOVA
Publication of US20220016002A1 publication Critical patent/US20220016002A1/en
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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • A61K8/342Alcohols having more than seven atoms in an unbroken chain
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q15/00Anti-perspirants or body deodorants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/046Aerosols; Foams
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • A61K8/345Alcohols containing more than one hydroxy group
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • A61K8/375Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/42Amides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/58Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
    • A61K8/585Organosilicon compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/20Chemical, physico-chemical or functional or structural properties of the composition as a whole
    • A61K2800/30Characterized by the absence of a particular group of ingredients
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59Mixtures
    • A61K2800/591Mixtures of compounds not provided for by any of the codes A61K2800/592 - A61K2800/596

Definitions

  • the present invention is in the field of cosmetic compositions and their use as antiperspirants, in particular, non-aluminium antiperspirant compositions.
  • EP 550,960 A1 (Unilever, 1992) discloses the use as an antiperspirant active of an amphiphilic material which forms, upon contact with perspiration, a water-insoluble liquid crystal phase of greater than one dimensional periodicity. This publication does not disclose ethanolic compositions, nor their stability issues.
  • WO 94/024993 discloses an antiperspirant composition
  • an amphiphilic material which forms, upon contact with perspiration, a water-insoluble liquid crystal phase of greater than one dimensional periodicity, in a cosmetic vehicle comprising a volatile silicone and containing less than 10% by weight of the total composition of a short chain monohydric alcohol.
  • composition that has a high degree of storage stability and that delivers skin care benefits.
  • an antiperspirant composition comprising ethanol, amphiphilic material, volatile silicone and a humectant, the amphiphilic material being a mixture consisting of glycerol monolaurate and isostearyl alcohol at a ratio of from 25:75 to 45:, wherein:
  • an antiperspirant aerosol composition comprising the addition of propellant to a composition according to the first aspect of the invention.
  • a cosmetic method of attaining an antiperspirant benefit comprising the topical application of a composition according to the first aspect of the invention.
  • ambient conditions refers to 20° C. and 1 atmosphere pressure, unless otherwise indicated.
  • cosmetic methods and compositions should be understood to mean non-therapeutic methods and compositions, respectively.
  • an “amphiphilic material” is a material defined by having both hydrophilic and hydrophobic portions in its structure.
  • water-insoluble means having a solubility in water of less than 0.1% by weight (at 37° C.).
  • Antiperspirant compositions according to the present invention are preferably free of aluminium or zirconium antiperspirant salts. Indeed, they are more preferably free of any aluminium or zirconium salts.
  • free of means having less 0.1% and preferably less than 0.01% of the specified component or components.
  • a “volatile silicone” is a silicone having a vapour pressure of greater than 1 Pa at 25° C.
  • compositions of the invention are particularly effectively when applied to the underarm regions of the human body and/or the feet.
  • the compositions are especially effectively when applied to the underarm regions of the human body.
  • Antiperspirant aerosol compositions consist of a propellant and a base.
  • the components of the base are typically mixed together first and the propellant is added last in a process sometimes called “gassing”. It is important that the base has good storage stability because there can be a significant period between the preparation of the base and the addition of the propellant.
  • the “base” of an antiperspirant aerosol composition is all the components of the total composition other than the propellant.
  • the fully formulated antiperspirant composition has good storage stability, so that it can survive prolonged transit to stores and extended periods on shelf prior to purchase and use.
  • the amphiphilic material is a mixture consisting of glycerol monolaurate and isostearyl alcohol at a ratio of from 25 75 to 45:55
  • amphiphilic material is at least 10% of the tri-component mixture consisting of ethanol, amphiphilic material and volatile siloxane.
  • the ratio of amphiphilic material to (ethanol+volatile silicone) is from 1:9 to 2:3, this ratio being alternatively stated as being from 10:90 to 40:60.
  • the amount of amphiphilic material in the tri-component mixture consisting of ethanol, amphiphilic material and volatile siloxane is from 10% to 40%.
  • amphiphilic material serves as the antiperspirant active for the composition, just as in the prior publications EP 550,960 A1 and WO 94/024993 by Unilever.
  • the amphiphilic material physically swells and forms a liquid crystal structure on contact with perspiration, hence enhancing the pore-blocking effect.
  • the content of the amphiphilic material in the total composition, ignoring any propellant therein, is preferably at least 10%, more preferably at least 12% and most preferably at least 15%.
  • the volatile silicone and its level of incorporation serves to reduce potential irritation and/or promote the good sensory properties of the composition.
  • the ratio of volatile silicone to (ethanol+amphiphilic material) in compositions of the invention is from 1:9 to 11:9, alternatively expressed as from 10:90 to 55:45. This equates to the volatile silicone being present at from 10% to 55% of the tri-component mixture consisting of ethanol, amphiphilic material and volatile siloxane. Preferably, the volatile silicone is present at from 10% to 50% and more preferably at from 15 to 40% of the tri-component mixture consisting of ethanol, amphiphilic material and volatile siloxane.
  • the content of volatile silicone in the total composition is preferably from 10% to 67%, more preferably from 10% to 50% most preferably from 15% to 40%.
  • the volatile silicone comprises greater than 90% by weight of, or consists of siloxanes having from 2 to 6 silicone atoms, arranged in either a cyclic or linear fashion.
  • the volatile silicone comprises greater than 90% by weight of, or consists of, siloxanes selected from the group consisting of hexamethyldisiloxane, octamethyltrisiiloxane, decamethyltetrasiloxane, dodecamethylpentasiloxane and decamethylcyclopentasiloxane.
  • the volatile silicone comprises greater than 90% by weight of, or consists of, siloxanes selected from the group consisting of hexamethyldisiloxane, octamethyltrisiiloxane, decamethyltetrasiloxane and decamethylcyclopentasiloxane.
  • Ethanol is an essential component of compositions of the invention, serving to aid the solubilisation of the amphiphilic material.
  • the ratio of ethanol to (amphiphilic material+volatile silicone) is from 3:7 to 3:2, alternative expressed as from 30:70 to 60:40. This equates to ethanol being present at from 30 to 60% of the tri-component mixture consisting of ethanol, amphiphilic material and volatile silicone.
  • the ratio of ethanol to amphiphilic material is at least 10:7. More preferably this ratio is at least 2:1 or 67:33.
  • the content of ethanol in the total composition, ignoring any propellant therein, is preferably at least 30%, more preferably at least 33% and most preferably at least 35%.
  • a humectant is an essential component of compositions od the invention.
  • Humectants used in the present invention are hygroscopic materials having the ability to form hydrogen-bonds.
  • the purpose of the humectant is to aid skin care by retaining moisture in the skin. This can improve the barrier properties of the skin.
  • Preferred humectants for use in the present invention have multiple hydrophilic groups, in particular hydroxyl groups and/or amine groups. Such materials can be particularly effective hydrogen-bond donors making them particular good humectants.
  • amine groups include such groups linked to a carbonyl group to form an amide, whether part of larger functional group or not.
  • humectants are selected from glycerol, 2-hydroxyethyl urea (HEU) and propylene glycol (PG).
  • humectants are polyhydroxylated materials like PG, dipropylene glycol (DPG) and glycerol.
  • An especially preferred humectant is glycerol.
  • the total amount of humectant used is from 0.1 to 10%, excluding any propellant that may be present. This level is preferably from 0.5 to 6% and more preferably from 1 to 5% of the composition excluding any propellant that may be present.
  • Humectants have been difficult to incorporate into conventional antiperspirant compositions comprising aluminium and zirconium antiperspirant salts. We have found that they can be incorporated into the alternative antiperspirant compositions of the present invention by careful selection of the amounts and ratios of components. Without such selection, multiphasic or unstable compositions result.
  • the composition is an antiperspirant aerosol composition comprising a propellant.
  • the propellant preferably comprises from 35 to 95% of the total composition, more preferably from 40 to 90% and most preferably from 50 to 85% of the total composition.
  • the propellant is commonly either a compressed gas or a material that boils at below ambient temperature, preferably at below 0° C., and especially at below ⁇ 10° C.
  • compressed gasses include nitrogen and carbon dioxide.
  • low boiling point materials include dimethyl ether.
  • Other possible low boiling point materials that may be used as propellants are hydrofluorocarbons containing from 2 to 4 carbons, at least one hydrogen and 3 to 7 fluorine atoms.
  • the propellant used comprises dimethyl ether or hydrocarbon.
  • compositions according to the invention are aerosol compositions, they can be made in a conventional manner by first preparing a base composition, charging the base composition into the aerosol can, fitting a valve assembly into the mouth of the can, thereby sealing the can, and thereafter charging propellant into the can to a desired pressure, and finally fitting an actuator on or over the valve assembly.
  • compositions of the invention is a deodorant active.
  • deodorant active typically antimicrobial agents active against bacterial on the skin of the human body. These serve to reduce malodour and especially useful in compositions in which the amphiphilic material is not itself an antimicrobial agent.
  • the level of incorporation is preferably 0.01%-5%, more preferably from 0.01-2% and most preferably from 0.03%-0.5% by weight of the total composition.
  • Preferred anti-microbial deodorant agents are those that are more efficacious than simple alcohols such as ethanol.
  • Particularly preferred anti-microbial deodorant agents are soluble in ethanol, meaning that they a solubility in ethanol of at least 10 g/L at 20° C.
  • Suitable anti-microbial deodorant agents include niacinamide; quaternary ammonium compounds, like cetyltrimethylammonium salts; chlorhexidine and salts thereof; and diglycerol monocaprate, diglycerol monolaurate, glycerol monolaurate, and similar materials, as described in “Deodorant Ingredients”, S. A. Makin and M. R. Lowry, in “Antiperspirants and Deodorants”, Ed. K. Laden (1999, Marcel Dekker, New York).
  • polyhexamethylene biguanide salts also known as polyaminopropyl biguanide salts
  • an example being Cosmocil CQ available from Arch Chemicals, 2′,4,4′-trichloro,2-hydroxy-diphenyl ether (triclosan), 3,7,11-trimethyldodeca-2,6,10-trienol (farnesol), essential oils such as Tea Tree Oil and Thyme Oil, climbazole, octapyrox, ketoconazole, zinc pyrithione and mixtures thereof.
  • a preferred optional component is a preservative, such as ethyl or methyl parabens or BHT (butyl hydroxy toluene), typically in an amount of from 0.01 to 0.1% by weight of the total composition.
  • a preservative such as ethyl or methyl parabens or BHT (butyl hydroxy toluene)
  • amphiphilic material used in these examples is designated as “lipid” and was a 60:40 blend of glycerol monolaurate and isostearyl alcohol.
  • the ethanol used in these examples was absolute alcohol.
  • the volatile silicone used in these examples was either DC200 or a 15:85 mix of DC245 and DC200, referred to in Table 1 as “Mix”.
  • humectants used in these examples were hydroxyethyl urea (HEU), propylene glycol (PG) and glycerol.
  • compositions indicated in Table 1 were prepared by methods known in the art.
  • the stability of the examples 5 to 8 and 12 to 15 was monitored for 8 weeks at 20° C.
  • the stability of all of the other examples and comparative examples was monitored for 4 weeks at ambient temperature.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Cosmetics (AREA)
US17/297,836 2018-11-30 2019-10-23 Non-aluminium antiperspirant compositions Pending US20220016002A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP18209520.8 2018-11-30
EP18209520 2018-11-30
PCT/EP2019/078941 WO2020108885A1 (en) 2018-11-30 2019-10-23 Non-aluminium antiperspirant compositions

Publications (1)

Publication Number Publication Date
US20220016002A1 true US20220016002A1 (en) 2022-01-20

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US17/297,836 Pending US20220016002A1 (en) 2018-11-30 2019-10-23 Non-aluminium antiperspirant compositions

Country Status (10)

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US (1) US20220016002A1 (es)
EP (1) EP3886796A1 (es)
CN (1) CN113164351A (es)
AU (1) AU2019389075B2 (es)
BR (1) BR112021008466A2 (es)
EA (1) EA202190945A1 (es)
MX (1) MX2021006190A (es)
PH (1) PH12021550980A1 (es)
WO (2) WO2020108886A1 (es)
ZA (1) ZA202103148B (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2022420330A1 (en) 2021-12-22 2024-06-13 Unilever Global Ip Limited Cosmetic sweat management compositions
WO2023117481A1 (en) 2021-12-22 2023-06-29 Unilever Ip Holdings B.V. Cosmetic sweat management compositions
WO2023117480A1 (en) 2021-12-22 2023-06-29 Unilever Ip Holdings B.V. Cosmetic sweat management compositions

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0251679A2 (en) * 1986-06-30 1988-01-07 Dow Corning Corporation Stick vehicle for skin care substances
US4822602A (en) * 1987-04-29 1989-04-18 The Procter & Gamble Company Cosmetic sticks
US20020146376A1 (en) * 2001-02-01 2002-10-10 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Cosmetic products for the reduction of sweat acidity

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3068546D1 (en) * 1979-11-07 1984-08-16 Procter & Gamble Antiperspirant compositions
DE3740186A1 (de) * 1987-06-24 1989-01-05 Beiersdorf Ag Desodorierende und antimikrobielle zusammensetzung zur verwendung in kosmetischen oder topischen zubereitungen
CA2082561A1 (en) 1991-11-12 1993-05-13 Francis J. Leng Antiperspirant materials and compositions
GB2273872A (en) * 1992-12-22 1994-07-06 Unilever Plc A method of treating skin
AU6679894A (en) 1993-04-30 1994-11-21 Unilever Plc Antiperspirant compositions
GB9502495D0 (en) * 1995-02-09 1995-03-29 Unilever Plc Antiperspirant compositions
GB0516418D0 (en) * 2005-08-10 2005-09-14 Unilever Plc Antiperspirant compositions
US20090130042A1 (en) * 2007-11-16 2009-05-21 Conopco, Inc., D/B/A Unilever Topical composition
CA2738683C (en) * 2008-10-23 2013-11-26 The Procter & Gamble Company Anhydrous antiperspirant compositions

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0251679A2 (en) * 1986-06-30 1988-01-07 Dow Corning Corporation Stick vehicle for skin care substances
US4822602A (en) * 1987-04-29 1989-04-18 The Procter & Gamble Company Cosmetic sticks
US20020146376A1 (en) * 2001-02-01 2002-10-10 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Cosmetic products for the reduction of sweat acidity

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
245 Fluid Material Safety Data Sheet (Year: 2006) *
Octamethylcyclotetrasiloxane Material Safety Data Sheet (Year: 2014) *
SF 1202 Material Safety Data Sheet (Year: 2003) *

Also Published As

Publication number Publication date
PH12021550980A1 (en) 2021-11-08
ZA202103148B (en) 2022-10-26
CN113164351A (zh) 2021-07-23
EP3886796A1 (en) 2021-10-06
WO2020108886A1 (en) 2020-06-04
BR112021008466A2 (pt) 2021-08-03
MX2021006190A (es) 2021-06-30
AU2019389075B2 (en) 2023-05-11
EA202190945A1 (ru) 2021-09-27
WO2020108885A1 (en) 2020-06-04
AU2019389075A1 (en) 2021-05-27

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